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You searched for subject:(Atropisomers). Showing records 1 – 13 of 13 total matches.

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University of Manchester

1. Staniland, Samantha Louise. Biocatalytic asymmetric synthesis of biaryl atropisomers.

Degree: 2016, University of Manchester

 Biaryl atropisomers are common structural motifs in natural products but most importantly they are used as chiral ligands in asymmetric catalysis. Despite their utility, current… (more)

Subjects/Keywords: Biocatalysis; Atropisomers

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Staniland, S. L. (2016). Biocatalytic asymmetric synthesis of biaryl atropisomers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297647

Chicago Manual of Style (16th Edition):

Staniland, Samantha Louise. “Biocatalytic asymmetric synthesis of biaryl atropisomers.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297647.

MLA Handbook (7th Edition):

Staniland, Samantha Louise. “Biocatalytic asymmetric synthesis of biaryl atropisomers.” 2016. Web. 17 Apr 2021.

Vancouver:

Staniland SL. Biocatalytic asymmetric synthesis of biaryl atropisomers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297647.

Council of Science Editors:

Staniland SL. Biocatalytic asymmetric synthesis of biaryl atropisomers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:297647


University of Manchester

2. Staniland, Samantha. Biocatalytic asymmetric synthesis of biaryl atropisomers.

Degree: PhD, 2016, University of Manchester

 Biaryl atropisomers are common structural motifs in natural products but most importantly they are used as chiral ligands in asymmetric catalysis. Despite their utility, current… (more)

Subjects/Keywords: 547; Biocatalysis; Atropisomers

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APA (6th Edition):

Staniland, S. (2016). Biocatalytic asymmetric synthesis of biaryl atropisomers. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/biocatalytic-asymmetric-synthesis-of-biaryl-atropisomers(fca72ad2-550c-4116-9d04-d63be929ea95).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728105

Chicago Manual of Style (16th Edition):

Staniland, Samantha. “Biocatalytic asymmetric synthesis of biaryl atropisomers.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 17, 2021. https://www.research.manchester.ac.uk/portal/en/theses/biocatalytic-asymmetric-synthesis-of-biaryl-atropisomers(fca72ad2-550c-4116-9d04-d63be929ea95).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728105.

MLA Handbook (7th Edition):

Staniland, Samantha. “Biocatalytic asymmetric synthesis of biaryl atropisomers.” 2016. Web. 17 Apr 2021.

Vancouver:

Staniland S. Biocatalytic asymmetric synthesis of biaryl atropisomers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Apr 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/biocatalytic-asymmetric-synthesis-of-biaryl-atropisomers(fca72ad2-550c-4116-9d04-d63be929ea95).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728105.

Council of Science Editors:

Staniland S. Biocatalytic asymmetric synthesis of biaryl atropisomers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/biocatalytic-asymmetric-synthesis-of-biaryl-atropisomers(fca72ad2-550c-4116-9d04-d63be929ea95).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.728105


University of Adelaide

3. Brusnahan, Jason Stewart. Total synthesis of ancistrotanzanine A.

Degree: 2010, University of Adelaide

 This thesis describes the first total synthesis of ancistrotanzanine A, a member of the naphthylisoquinoline class of natural products. In Chapter 1 the synthetic challenges… (more)

Subjects/Keywords: naphthylisoquinoline alkaloids; isoquinoline; natural products; atropisomers; biaryl

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APA (6th Edition):

Brusnahan, J. S. (2010). Total synthesis of ancistrotanzanine A. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/60142

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Brusnahan, Jason Stewart. “Total synthesis of ancistrotanzanine A.” 2010. Thesis, University of Adelaide. Accessed April 17, 2021. http://hdl.handle.net/2440/60142.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Brusnahan, Jason Stewart. “Total synthesis of ancistrotanzanine A.” 2010. Web. 17 Apr 2021.

Vancouver:

Brusnahan JS. Total synthesis of ancistrotanzanine A. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2440/60142.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Brusnahan JS. Total synthesis of ancistrotanzanine A. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/60142

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

4. Oketani, Ryusei. Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization.

Degree: Docteur es, Chimie, 2019, Normandie

Les techniques de séparation chirale sont importantes pour permettre des études relatives de l’activité biologique des molécules chirales. Dans cette thèse, la séparation chirale des… (more)

Subjects/Keywords: Déracémisation; Atropisomères; Cristallisation; Deracemization; Atropisomers; Crystallization; 547.7

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APA (6th Edition):

Oketani, R. (2019). Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2019NORMR109

Chicago Manual of Style (16th Edition):

Oketani, Ryusei. “Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization.” 2019. Doctoral Dissertation, Normandie. Accessed April 17, 2021. http://www.theses.fr/2019NORMR109.

MLA Handbook (7th Edition):

Oketani, Ryusei. “Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization.” 2019. Web. 17 Apr 2021.

Vancouver:

Oketani R. Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization. [Internet] [Doctoral dissertation]. Normandie; 2019. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2019NORMR109.

Council of Science Editors:

Oketani R. Aspects pratiques de la déracémisation d'atropisomères par cristallisation : Practical aspects on how to deracemize atropizomers by means of crystallization. [Doctoral Dissertation]. Normandie; 2019. Available from: http://www.theses.fr/2019NORMR109


University of Toronto

5. Diaz, Diego Benjamin. Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules.

Degree: PhD, 2020, University of Toronto

 Conformation describes the spatial arrangement of atoms in a molecule. While the binding energy between atoms in a molecule determines its structure, the three-dimensional geometry… (more)

Subjects/Keywords: Aminoboronic acids; Atropisomers; Boron; Conformational analysis; Macrocycles; Peptides; 0485

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APA (6th Edition):

Diaz, D. B. (2020). Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/101248

Chicago Manual of Style (16th Edition):

Diaz, Diego Benjamin. “Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules.” 2020. Doctoral Dissertation, University of Toronto. Accessed April 17, 2021. http://hdl.handle.net/1807/101248.

MLA Handbook (7th Edition):

Diaz, Diego Benjamin. “Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules.” 2020. Web. 17 Apr 2021.

Vancouver:

Diaz DB. Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules. [Internet] [Doctoral dissertation]. University of Toronto; 2020. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1807/101248.

Council of Science Editors:

Diaz DB. Identification of Novel Structural Motifs for Mining the Conformational Space of Boron- and Peptide-based Molecules. [Doctoral Dissertation]. University of Toronto; 2020. Available from: http://hdl.handle.net/1807/101248


Universidade Estadual de Campinas

6. Andrade, Yuri Ferreira dos Santos, 1992-. Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol.

Degree: Instituto de Química; Programa de Pós-Graduação em Química, 2017, Universidade Estadual de Campinas

Orientador: Jackson Dirceu Megiatto Junior

Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Química

Made available in DSpace on 2018-10-18T13:07:07Z (GMT). No. of bitstreams:… (more)

Subjects/Keywords: Porfirinas; Forças intermoleculares; Atropoisômeros; Porphyrins; Intermolecular forces; Atropisomers

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APA (6th Edition):

Andrade, Yuri Ferreira dos Santos, 1. (2017). Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol. (Masters Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/332561

Chicago Manual of Style (16th Edition):

Andrade, Yuri Ferreira dos Santos, 1992-. “Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol.” 2017. Masters Thesis, Universidade Estadual de Campinas. Accessed April 17, 2021. http://repositorio.unicamp.br/jspui/handle/REPOSIP/332561.

MLA Handbook (7th Edition):

Andrade, Yuri Ferreira dos Santos, 1992-. “Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol.” 2017. Web. 17 Apr 2021.

Vancouver:

Andrade, Yuri Ferreira dos Santos 1. Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol. [Internet] [Masters thesis]. Universidade Estadual de Campinas; 2017. [cited 2021 Apr 17]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332561.

Council of Science Editors:

Andrade, Yuri Ferreira dos Santos 1. Investigation of the secondary interactions in phenol-functionalized porphyrin atropisomers : Investigação de interações secundárias em atropoisômeros porfirínicos funcionalizados com fenol. [Masters Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/332561

7. Belot, Vincent. Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents.

Degree: Docteur es, Sciences chimiques. Chimie organique, 2017, Aix Marseille Université

Une échelle de taille contenant 20 substituants usuels en chimie a été construite à partir des barrières de rotations de N-aryl-thiazoline-2-thiones. L’énergie d’activation ΔG≠rot qui… (more)

Subjects/Keywords: Échelle de taille; Atropisomères; Stéréochimie dynamique; HPLC chirale; Size scale; Atropisomers; Dynamic stereochemistry; Chiral HPLC

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Belot, V. (2017). Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0408

Chicago Manual of Style (16th Edition):

Belot, Vincent. “Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed April 17, 2021. http://www.theses.fr/2017AIXM0408.

MLA Handbook (7th Edition):

Belot, Vincent. “Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents.” 2017. Web. 17 Apr 2021.

Vancouver:

Belot V. Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2017AIXM0408.

Council of Science Editors:

Belot V. Accès à une bibliothèque ciblée de n-aryl-thiazoline-2-thiones pour l'établissement d'une nouvelle échelle de taille de substituants usuels : Access to a targeted library of n-aryl-thiazoline-2-thiones for the establishment of a new size scale of common substituents. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0408

8. Sidi Boune, Mohamed Vall. Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav.

Degree: Docteur es, Chimie organique, minérale et industrielle, 2019, Normandie; Université de Nouakchott

Cette thèse décrit une méthodologie innovante d’extraction et d’hémisynthèse simultanée, dénommée SECheM (Simultaneous Extraction and Chemical Modification) sur une plante mauritanienne le Cienfuegosia digitata Cav.… (more)

Subjects/Keywords: Gossypol; Cienfuegosia digitata cav.; Malvaceae; Bases de Schiff; Atropoisomères; SECheM; Izide; Réaction d'échange d'amine; Atropisomers; Bases of Schiff; Amine exchange reaction

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APA (6th Edition):

Sidi Boune, M. V. (2019). Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav. (Doctoral Dissertation). Normandie; Université de Nouakchott. Retrieved from http://www.theses.fr/2019NORMLH03

Chicago Manual of Style (16th Edition):

Sidi Boune, Mohamed Vall. “Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav.” 2019. Doctoral Dissertation, Normandie; Université de Nouakchott. Accessed April 17, 2021. http://www.theses.fr/2019NORMLH03.

MLA Handbook (7th Edition):

Sidi Boune, Mohamed Vall. “Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav.” 2019. Web. 17 Apr 2021.

Vancouver:

Sidi Boune MV. Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav. [Internet] [Doctoral dissertation]. Normandie; Université de Nouakchott; 2019. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2019NORMLH03.

Council of Science Editors:

Sidi Boune MV. Valorisation en synthèse organique des phytoconstituants (dérivés du gossypol) extraits de Cienfuegosia Digitata. Cav : Valorization in organic synthesis of phytoconstituents (Gossypol derivatives) extracted from Cienfuegosia Digita. Cav. [Doctoral Dissertation]. Normandie; Université de Nouakchott; 2019. Available from: http://www.theses.fr/2019NORMLH03


University of Otago

9. Feng, Feifei. In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system .

Degree: University of Otago

 Ketotifen (K) is a first-generation antihistamine with antiinflammatory potency. It penetrates the blood-brain barrier (BBB) and causes a sedative side effect. Norketotifen (N) is an… (more)

Subjects/Keywords: Ketotifen; Norketotifen; Atropisomers; Sedation; H1; receptor; binding; H1 receptor binding

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APA (6th Edition):

Feng, F. (n.d.). In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/10015

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Feng, Feifei. “In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system .” Doctoral Dissertation, University of Otago. Accessed April 17, 2021. http://hdl.handle.net/10523/10015.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Feng, Feifei. “In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system .” Web. 17 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Feng F. In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system . [Internet] [Doctoral dissertation]. University of Otago; [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10523/10015.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Feng F. In vitro and in vivo studies on the binding and permeation of ketotifen and norketotifen atropisomers in the central nervous system . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/10015

Note: this citation may be lacking information needed for this citation format:
No year of publication.

10. Quinonero, Ophélie. Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin.

Degree: Docteur es, Chimie Organique, 2016, Aix Marseille Université

Ces travaux de thèse ont porté sur le développement d’une méthodologie de conversion de chiralité centrale vers axiale pour la formation de 4-arylpyridines atropoisomères, et… (more)

Subjects/Keywords: 1; 4-Dihydropyridines; 4-Arylpyridines; Atropoisomères; Organocatalyse; Conversion de chiralité; Synthèse totale; (+)-Streptonigrine; 1; 4-Dihydropyridines; 4-Arylpyridines; Atropisomers; Organocatalysis; Chirality conversion; Total synthesis; (+)-Streptonigrin

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APA (6th Edition):

Quinonero, O. (2016). Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4350

Chicago Manual of Style (16th Edition):

Quinonero, Ophélie. “Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed April 17, 2021. http://www.theses.fr/2016AIXM4350.

MLA Handbook (7th Edition):

Quinonero, Ophélie. “Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin.” 2016. Web. 17 Apr 2021.

Vancouver:

Quinonero O. Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2016AIXM4350.

Council of Science Editors:

Quinonero O. Synthèse organocatalysée énantiosélective de 4-arylpyridines atropoisomères par conversion de chiralité centrale à axiale : application vers la synthèse totale de la streptonigrine : Enantioselective organocatalysed synthesis of 4-arylpyridine atropisomers by central-to-axial chirality conversion : application towards the total synthesis of (+)-streptonigrin. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4350

11. Doulain, Pierre-Emmanuel. Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics.

Degree: Docteur es, Chimie, 2015, Université de Bourgogne

Ce travail décrit de nouveaux composés thérapeutiques anticancéreux traçables par imagerie optique appelés théranostiques optiques.Après un premier chapitre bibliographique décrivant le contexte de l’imagerie et… (more)

Subjects/Keywords: Imagerie optique; BODIPY; Atropoisomères; Théranostique; Phosphine-or; Picket-Fence; Études in vitro; Proche infra-rouge; Agrégation; Photoacoustique; Optical Imaging; BODIPY; Atropisomers; Theranostic; Phosphine-Gold; Picket Fence; In vitro studies; Near-infrared; Aggregation; Photoacoustic; 540; 610.2

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APA (6th Edition):

Doulain, P. (2015). Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics. (Doctoral Dissertation). Université de Bourgogne. Retrieved from http://www.theses.fr/2015DIJOS036

Chicago Manual of Style (16th Edition):

Doulain, Pierre-Emmanuel. “Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics.” 2015. Doctoral Dissertation, Université de Bourgogne. Accessed April 17, 2021. http://www.theses.fr/2015DIJOS036.

MLA Handbook (7th Edition):

Doulain, Pierre-Emmanuel. “Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics.” 2015. Web. 17 Apr 2021.

Vancouver:

Doulain P. Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics. [Internet] [Doctoral dissertation]. Université de Bourgogne; 2015. [cited 2021 Apr 17]. Available from: http://www.theses.fr/2015DIJOS036.

Council of Science Editors:

Doulain P. Complexes de BODIPY - phosphine - or : application à la conception de théranostiques optiques : BODIPY - phosphane - gold complexes : towards the elaboration of optical theranostics. [Doctoral Dissertation]. Université de Bourgogne; 2015. Available from: http://www.theses.fr/2015DIJOS036


University of South Carolina

12. Zhang, Yagang. Molecularly Imprinted Polymers – New Insights and Strategies.

Degree: PhD, Chemistry and Biochemistry, 2010, University of South Carolina

  Solvent programmable polymers (SPPs) were developed based on restricted rotation with the ability to respond and remember the stimuli-induced properties. The SPP was prepared… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; atropisomers; functional monomer aggregation; functional monomer dimerization; molecular memory; molecularly imprinted polymers; stimuli-responsive materials

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zhang, Y. (2010). Molecularly Imprinted Polymers – New Insights and Strategies. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/299

Chicago Manual of Style (16th Edition):

Zhang, Yagang. “Molecularly Imprinted Polymers – New Insights and Strategies.” 2010. Doctoral Dissertation, University of South Carolina. Accessed April 17, 2021. https://scholarcommons.sc.edu/etd/299.

MLA Handbook (7th Edition):

Zhang, Yagang. “Molecularly Imprinted Polymers – New Insights and Strategies.” 2010. Web. 17 Apr 2021.

Vancouver:

Zhang Y. Molecularly Imprinted Polymers – New Insights and Strategies. [Internet] [Doctoral dissertation]. University of South Carolina; 2010. [cited 2021 Apr 17]. Available from: https://scholarcommons.sc.edu/etd/299.

Council of Science Editors:

Zhang Y. Molecularly Imprinted Polymers – New Insights and Strategies. [Doctoral Dissertation]. University of South Carolina; 2010. Available from: https://scholarcommons.sc.edu/etd/299


University of Newcastle

13. Trinh, Nguyen Trieu. Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents.

Degree: PhD, 2016, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

The HSP plays a pivotal role in the spatial and temporal regulation of cell proliferation and differentiation. Conversely… (more)

Subjects/Keywords: hedgehog signalling pathway inhibitors; Hh inhibitors; SW480 (colon carcinoma); MCF-7 (breast carcinoma); A2780 (ovarian carcinoma); H460 (lung carcinoma); DU145 (prostate carcinoma); BE2-C (neuroblastoma); MIA (pancreatic carcinoma); TCAM-2 (seminoma); Shh LIGHT2 (derived from NIH-3T3 fibroblast); dual luciferase reporter assay; GLI inhibitors; reverse transcription PCR (RT-PCR); quantitative PCR (qPCR) assays; MTT assay; SAG-induced Hh activation; Ugi-Knoevenagel three- and four-component products; quinolone-1-(2H)-ones; multicomponent reaction; 1,3-thiazine-6-phenylimino-5-carboxylates; isothiocyanate; 1,3-thiazine anhydride; SMO inhibitors; ethyl 3-aminocrotonate; L-tryptophan analogues; benzo[1,3]dioxol-5-ylmethyl-[2-(1H-indol-3-yl)-ethyl]-amines; 1D selective NOESY NMR experiment; variable temperature NMR experiment; atropisomerism; atropisomers; diastereoisomers; cancer suppressing agents; anti-cancer; PTCH inhibitors; flow chemistry; NVP-LDE225 (Sonidegib); catalyst leaching; FibreCats®; furanyl–biaryl based analogues; CatCart™; FC1032™; PdCl2(PPh3)2-DVB; Suzuki cross-couplings; catalyst leaching; Hh cancer cell lines; thesis by publication; GLI1; GLI2; GLI3; HT29

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Trinh, N. T. (2016). Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1337980

Chicago Manual of Style (16th Edition):

Trinh, Nguyen Trieu. “Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents.” 2016. Doctoral Dissertation, University of Newcastle. Accessed April 17, 2021. http://hdl.handle.net/1959.13/1337980.

MLA Handbook (7th Edition):

Trinh, Nguyen Trieu. “Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents.” 2016. Web. 17 Apr 2021.

Vancouver:

Trinh NT. Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents. [Internet] [Doctoral dissertation]. University of Newcastle; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1959.13/1337980.

Council of Science Editors:

Trinh NT. Small molecule inhibitors of the hedgehog signalling pathway as cancer suppressing agents. [Doctoral Dissertation]. University of Newcastle; 2016. Available from: http://hdl.handle.net/1959.13/1337980

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